FDA 510(k)

麗文拓壓力計，Soprano 10，Soprano

K 號：K192251 · 2020-01-15

決定日期2020-01-15

產品代碼EIH

諮詢委員會DE

決定相當於

器材摘要

Livento Press, Soprano 10, Soprano is the device name listed in this FDA 510(k) record. The listed applicant is Cendres+Metaux SA. It received FDA 510(k) clearance on 2020-01-15 under 510(k) number K192251. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Livento Press, Soprano 10, Soprano?

Livento Press, Soprano 10, Soprano is a medical device that received FDA 510(k) clearance on 2020-01-15. The listed applicant is Cendres+Metaux SA. The 510(k) number is K192251.

When did Livento Press, Soprano 10, Soprano receive FDA 510(k) clearance?

Livento Press, Soprano 10, Soprano received FDA 510(k) clearance on 2020-01-15, under 510(k) number K192251.

Who is the listed applicant for Livento Press, Soprano 10, Soprano?

The FDA 510(k) record lists Cendres+Metaux SA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Livento Press, Soprano 10, Soprano?

The FDA product code for Livento Press, Soprano 10, Soprano is EIH.

其他以 Cendres+Metaux SA 為申請人之記錄

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相關器械（代碼：EIH）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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